The evaluation of palatal augmentation prosthesis and palatal lift prosthesis on pharyngeal swallowing pressure by High-Resolution Manometry: before-after study
Not Applicable
- Conditions
- dysphagia
- Registration Number
- JPRN-UMIN000036446
- Lead Sponsor
- Hamamatsu City Rehabilitation Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up continuing
- Sex
- All
- Target Recruitment
- 20
Inclusion Criteria
Not provided
Exclusion Criteria
Patients who judged that the HRM evaluation was inappropriate or impossible Patients who are allergic to lidocaine Patients who cannot use the intraoral prosthesis at meal time Patient who use nasogastric tube for feeding during the HRM evaluation
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method pharyngeal swallowing pressure
- Secondary Outcome Measures
Name Time Method nutrition status Patient subjectivity swallowing function